Literature DB >> 22484535

[Extra medullary hematopoiesis associated to congenital dyserythropoietic anemia II in adult].

Inès Jedidi1, Moez Medhaffar, Manel Ghorbel, Sondes Hdiji, Faiza Makni, Moez Elloumi, Choumous Kallel.   

Abstract

The congenital dyserythropoietic anemias comprise a group of rare hereditary disorders of erythropoiesis characterized by anemia with ineffective erythropoiesis and morphological abnormalities of erythroblasts in the bone marrow. Congenital dyserythropoietic anemia type II or HEMPAS is the more frequent type. It is rare in adults. Extra medullary hematopoiesis is also a rare entity; it is a physiological response to chronic anemia observed in certain hemopathies like congenital dyserythropoietic anemia type II. We report the observation of a patient for who diagnosis of extra medullary hematopoiesis associated to congenital dyserythropoietic type II was made in adulthood.

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Year:  2012        PMID: 22484535     DOI: 10.1684/abc.2012.0694

Source DB:  PubMed          Journal:  Ann Biol Clin (Paris)        ISSN: 0003-3898            Impact factor:   0.459


  1 in total

1.  Paravertebral Mass and Diffuse Lymphadenopathy in a Patient with Pyruvate Kinase Deficiency: Malignancy or Alternative Etiology?

Authors:  Hira Shaikh; Veli Bakalov; Soorih Shaikh; Ali Amjad
Journal:  Cureus       Date:  2019-06-06
  1 in total

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